Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62436728-62437165 | Common:1; Rare:119 | ||||
chr1:62688266-62688541 | Common:1; Rare:106 | ||||
chr1:62784070-62784180 | Rare:44 | ||||
chr1:63367504-63367685 | Rare:53; Clinvar (benign):1 | ||||
chr1:63523186-63523595 | Common:3; Rare:102 | ||||
chr1:63593214-63593722 | Rare:215; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr1:63594208-63594257 | Common:1; Rare:11 | ||||
chr1:64744804-64744950 | Rare:47 | ||||
chr1:64841276-64841606 | Rare:75; Clinvar:2 | ||||
chr1:64966409-64966714 | Common:2; Rare:110 | ||||
chr1:65148025-65148318 | Common:5; Rare:59 | ||||
chr1:65148722-65149053 | Common:3; Rare:97 | ||||
chr1:66924757-66925068 | Common:2; Rare:135 | ||||
chr1:66925219-66925559 | Common:2; Rare:103 | ||||
chr1:66930088-66930411 | Rare:100 |